CITRULLINE-CONTAINING MYELIN BASIC-PROTEIN IS RECOGNIZED BY T-CELL LINES DERIVED FROM MULTIPLE-SCLEROSIS PATIENTS AND HEALTHY-INDIVIDUALS

被引:37
作者
MARTIN, R
WHITAKER, JN
RHAME, L
GOODIN, RR
MCFARLAND, HF
机构
[1] NINCDS, NEUROIMMUNOL BRANCH, BETHESDA, MD USA
[2] VET AFFAIRS MED CTR, NEUROL SERV, BIRMINGHAM, AL USA
[3] VET AFFAIRS MED CTR, RES SERV, BIRMINGHAM, AL USA
[4] UNIV ALABAMA, DEPT NEUROL, BIRMINGHAM, AL 35294 USA
关键词
D O I
10.1212/WNL.44.1.123
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The cause of MS is uncertain, but an autoimmune disorder of the CNS is likely, and myelin basic protein (MBP) is a candidate antigen. MBP exists in different isoforms, generated by differential splicing of exons, and in charge isomers, generated by posttranslational modifications. Different isoforms and charge isomers presumably subserve different functions, and they vary in abundance in immature myelin found during myelinogenesis and remyelination compared with mature myelin. The 18.5-kd isomer is most abundant in normal human adults and consequently has been used almost exclusively for immunologic studies in MS. In the present study, we examined a different but abundant charge isomer of MBP, termed MBP-C8, to determine whether it could be recognized by MBP-specific cytotoxic and proliferative T-cell lines (TCL) and whether a T-cell response directed exclusively against citrulline-containing residues of MBP-C8 exists in MS patients and healthy controls. We showed that citrulline affects antigen recognition by some TCL that are specific for areas of MBP that contain the citrulline residues. Following stimulation with MBP-C8, MBP-C8-specific TCL could be generated from both MS patients and controls. T-cell responses against antigens that appear during myelinogenesis and during remyelination may be important in inducing and perpetuating an autoimmune response involved in the pathogenesis of MS.
引用
收藏
页码:123 / 129
页数:7
相关论文
共 37 条
[1]  
BRODSKY FM, 1991, ANNU REV IMMUNOL, V9, P707
[2]   MOLECULAR-BIOLOGY OF MYELIN PROTEINS FROM THE CENTRAL NERVOUS-SYSTEM [J].
CAMPAGNONI, AT .
JOURNAL OF NEUROCHEMISTRY, 1988, 51 (01) :1-14
[3]   RESPONSE OF HUMAN LYMPHOCYTE-T LINES TO MYELIN BASIC-PROTEIN - ASSOCIATION OF DOMINANT EPITOPES WITH HLA CLASS-II RESTRICTION MOLECULES [J].
CHOU, YK ;
VAINIENE, M ;
WHITHAM, R ;
BOURDETTE, D ;
CHOU, CHJ ;
HASHIM, G ;
OFFNER, H ;
VANDENBARK, AA .
JOURNAL OF NEUROSCIENCE RESEARCH, 1989, 23 (02) :207-216
[4]   FREQUENCY OF T-CELLS SPECIFIC FOR MYELIN BASIC-PROTEIN AND MYELIN PROTEOLIPID PROTEIN IN BLOOD AND CEREBROSPINAL-FLUID IN MULTIPLE-SCLEROSIS [J].
CHOU, YK ;
BOURDETTE, DN ;
OFFNER, H ;
WHITHAM, R ;
WANG, RY ;
HASHIM, GA ;
VANDENBARK, AA .
JOURNAL OF NEUROIMMUNOLOGY, 1992, 38 (1-2) :105-113
[5]   BINDING OF HUMAN NORMAL AND MULTIPLE-SCLEROSIS DERIVED MYELIN BASIC-PROTEIN TO PHOSPHOLIPID-VESICLES - EFFECTS ON MEMBRANE HEAD GROUP AND BILAYER REGIONS [J].
DEBER, CM ;
HUGHES, DW ;
FRASER, PE ;
PAWAGI, AB ;
MOSCARELLO, MA .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1986, 245 (02) :455-463
[6]  
DEIBLER GE, 1973, J BIOL CHEM, V248, P2392
[7]   LARGE-SCALE PREPARATION OF MYELIN BASIC PROTEIN FROM CENTRAL NERVOUS-TISSUE OF SEVERAL MAMMALIAN SPECIES [J].
DEIBLER, GE ;
KIES, MW ;
MARTENSON, RE .
PREPARATIVE BIOCHEMISTRY, 1972, 2 (02) :139-+
[8]   PEPTIDE MHC INTERACTION IN AUTOIMMUNITY [J].
FAIRCHILD, PJ ;
WRAITH, DC .
CURRENT OPINION IN IMMUNOLOGY, 1992, 4 (06) :748-753
[9]   MYELIN BASIC-PROTEIN IS AFFECTED BY REDUCED SYNTHESIS OF MYELIN PROTEOLIPID PROTEIN IN THE JIMPY MOUSE [J].
FANNON, AM ;
MOSCARELLO, MA .
BIOCHEMICAL JOURNAL, 1990, 268 (01) :105-110
[10]  
FRITZ RB, 1989, CHEM IMMUNOL, V46, P101